Sexuality Clinical Trial
— ENFOCATEOfficial title:
Study Protocol: a Randomized Controlled Trial of a Gender-transformative School-based Sexual Health Intervention in Chilean Students
The goal of this randomized controlled trial (RCT) is to evaluate the effectiveness of a comprehensive gender-transformative intervention of sexual education (ENFOCATE -Focus-on) in adolescents, using a mixed experimental design. The intervention will be directed exclusively to students of the 10th and 11th grades who are enrolled in one of the education establishments that depend on the Municipality of Santiago. The randomization will be by grade, and the data will be collected at three moments (pre-intervention, post-intervention and a 3-month follow-up).
Status | Not yet recruiting |
Enrollment | 609 |
Est. completion date | December 29, 2023 |
Est. primary completion date | September 3, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 14 Years to 16 Years |
Eligibility | Inclusion Criteria - Schools with students of the 10th and 11th grades who are enrolled in one of the education establishments that depend on the Municipality of Santiago. - Schools not being an education center oriented to adults or persons deprived of liberty (e.g. closed or semi-closed compounds of GendarmerÃa de Chile or the National Service for Minors) - Schools with regularity in teaching and learning (for example, schools that were not partially interrupted in 2022 by student manifestations) - Schools with informed consent of the director. - Students having 90% or greater attendance in classes - Students providing informed consent of voluntary participation - Students having explicit and informed consent of their parents or guardians. Exclusion Criteria: - Schools being an education center oriented to adults or persons deprived of liberty - Schools without informed consent of the director - Students without class attendance - Students without informed consent of voluntary participation - Students without an explicit and informed consent of their parents or guardians |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University of Chile | National Fund for Research and Development in Health, Chile |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in knowledge of sexuality | Related to information about the biological components of sexuality. The test used will be the Knowledge Test (KT). This is a 34-item multiple choice instrument which was designed to evaluate the knowledge on sexuality in adolescents; it evaluates areas including pregnancy, STI, physical development. Higher scores represent more favorable attitudes. Its reliability is a=0.89. These assessed areas will be combined to report the level of knowledge. | One-week pre-intervention, immediately post-intervention and a 3-month follow-up | |
Primary | Change in preventive sexual behavior | Related to behavior in sexuality and preventive behavior in sexuality. Ad-hoc survey. It will be elaborated by the research team to evaluate the behavior and intention, self-efficacy and empowerment in sexuality in LGTB and female-male students. Ad-hoc surveys have been used and reported in other RCT of interventions in sexual health. | One-week pre-intervention, immediately post-intervention and a 3-month follow-up | |
Primary | Change in gender actitude | Related to positive disposition towards persons of different genders. The test used will be the Scale for Detection of Sexism in adolescents (DSA). This is an instrument of 26 items developed for adolescents. It evaluates sexism, differentiating between hostile and benevolent sexism. The response scale for the items is a Likert type with six alternatives (from 1=disagree completely to 6=agree completely). Higher scores indicate more sexism. Its reliability is a= .881. | One-week pre-intervention, immediately post-intervention and a 3-month follow-up | |
Primary | Change in gender actitude | Related to positive disposition towards persons of different sexual orientation. The test used will be the Scale of negative attitudes toward trans persons (NATP). It measures attitude as an expression of prejudice towards trans persons. It has nine items with a Likert scale with five response options, from 1= disagree completely to 5=agree completely. Higher scores are indicators of higher levels of negative attitudes toward persons of different sexual orientation. Its reliability is a= .886. | One-week pre-intervention, immediately post-intervention and a 3-month follow-up | |
Primary | Change in gender actitude | Related to positive disposition towards persons of different sexual orientation. The test used will be the Short version of Modern Homophobia Scale (MHS). It measures homophobic attitudes in the dimension personal discomfort, institutional and deviation/changeability. It is composed of 46 items that evaluate attitudes towards lesbians and gay in a Likert scale of 1-5 in which higher scores interpret more positive attitudes towards homosexuality and lesbianism. Its reliability is a= .80. | One-week pre-intervention, immediately post-intervention and a 3-month follow-up | |
Primary | Change in components of mental health related to sexual health | Decrease of internalizing symptomology. The test used will be the Pediatric Symptom Checklist (PSC-17). It evaluates general psychosocial functioning, detecting emotional and behavioral difficulties in children and adolescents. Higher scores represent more internalizing behaviors. reliability is a= .72. | One-week pre-intervention, immediately post-intervention and a 3-month follow-up | |
Primary | Change in components of mental health related to sexual health | Decrease of externalizing symptomology. The test used will be the Pediatric Symptom Checklist (PSC-17). It evaluates general psychosocial functioning, detecting emotional and behavioral difficulties in children and adolescents. Higher scores represent more externalizing behaviors. Its reliability is a= .72. | One-week pre-intervention, immediately post-intervention and a 3-month follow-up |
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